骨质疏松症与痴呆风险之间的关系:一项以韩国妇女为基础的全国性队列研究。

IF 5.4
Min Young Chun, Jimin Jeon, Seok Jong Chung, Jinkwon Kim
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引用次数: 0

摘要

基本原理:痴呆症和骨质疏松症有共同的危险因素,并且在老龄化人口中呈上升趋势。主要结果:骨质疏松显著增加韩国老年妇女发生全因痴呆、阿尔茨海默病痴呆和血管性痴呆的风险。论文意义:早期发现和治疗骨质疏松症可降低痴呆风险。目的:痴呆和骨质疏松症具有共同的危险因素,并且在老龄化人群中的患病率正在上升。本研究旨在调查骨质疏松症对女性痴呆及其亚型的影响,使用基于人群的健康筛查队列数据,随访期超过10年。方法:对2010 ~ 2011年参加“国家过渡年龄筛查计划”的66岁韩国女性进行回顾性研究。根据脊柱骨密度t评分将参与者分为三组:正常组(t评分≥- 1.0标准差[SD];结果:该研究纳入了131872名66岁无痴呆的女性。在平均10.4±1.8年的随访中,9399人患上了全因痴呆(7.1%)。骨质疏松症与全因痴呆风险增加相关(调整亚分布风险比[asHR] 1.14;95%置信区间[CI] 1.08-1.21;结论:我们的研究结果强调了骨质疏松症与全因痴呆、AD痴呆和VaD风险增加之间的关联。早期发现和治疗骨质疏松症在预防痴呆中的作用有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between osteoporosis and risk of dementia: a Korean women nationwide population-based cohort study.

Brief rationale: dementia and osteoporosis share risk factors and are rising in aging populations.

Main results: osteoporosis significantly increases the risk of all-cause dementia, Alzheimer's disease dementia, and vascular dementia in Korean older women. Significance of the paper: early detection and treatment of osteoporosis may reduce dementia risk.

Purpose: Dementia and osteoporosis share common risk factors and are increasing in prevalence in the aging population. This study aimed to investigate the impact of osteoporosis on dementia and its subtypes in women using data from a population-based, health-screening cohort, with a follow-up period of more than 10 years.

Methods: This retrospective study included 66-year-old Korean women who participated in the "National Screening Program for Transitional Ages" from 2010 to 2011. Participants were categorized based on spine bone mineral density T-scores into three groups: normal (T-score ≥ - 1.0 standard deviation [SD]; 18.7%), osteopenia (- 2.5 SD < T-score < - 1.0 SD; 42.5%), and osteoporosis (T-score ≤ - 2.5 SD; 38.8%). Incident dementia cases were evaluated until 2021 using national healthcare claims databases. Fine-Gray subdistribution hazard models were used to assess the risks of all-cause dementia including Alzheimer's disease (AD) dementia and vascular dementia (VaD), accounting for death as a competing risk.

Results: The study included 131,872 dementia-free women aged 66 years. Over an average follow-up of 10.4 ± 1.8 years, 9399 individuals developed all-cause dementia (7.1%). Osteoporosis was associated with increased risks for all-cause dementia (adjusted subdistribution hazard ratio [asHR] 1.14; 95% confidence interval [CI] 1.08-1.21; p < 0.001), AD dementia (asHR 1.14; 95% CI 1.08-1.22; p < 0.001), and VaD (asHR 1.42; 95% CI 1.08-1.87; p = 0.013), compared to normal.

Conclusion: Our findings highlight an association between osteoporosis and increased risks of developing all-cause dementia, AD dementia, and VaD. Further research is needed to explore the effects of early identification and treatment of osteoporosis in preventing dementia.

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